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“Ambu” SPUR II Resuscitator - Taiwan Registration 03cbf4f1d7c8d97512b51184ad49a3eb

Access comprehensive regulatory information for “Ambu” SPUR II Resuscitator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 03cbf4f1d7c8d97512b51184ad49a3eb and manufactured by AMBU LIMITED;;AMBU A/S. The authorized representative in Taiwan is HWA YI MEDICAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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03cbf4f1d7c8d97512b51184ad49a3eb
Registration Details
Taiwan FDA Registration: 03cbf4f1d7c8d97512b51184ad49a3eb
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Device Details

“Ambu” SPUR II Resuscitator
TW: “安佈”思璞甦醒器
Risk Class 2
MD

Registration Details

03cbf4f1d7c8d97512b51184ad49a3eb

Ministry of Health Medical Device Land Transport No. 001051

DHA09200105105

Company Information

Denmark;;China

Product Details

For details, it is Chinese approved copy of the imitation order

D Devices for anesthesiology

D5915 Manual Emergency Respirator

Imported from abroad; Contract manufacturing;; Made in China

Dates and Status

Jul 22, 2019

Jul 22, 2024